Magnesium Schiff Base Catalyzed Direct Asymmetric Aldol Reaction

Several novel chiral Schiff base ligands were prepared from a commercially available chloramphenicol base and applied to the titanium-mediated asymmetric aldol reaction of diketene with various α,β-unsaturated aldehydes.

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Direct catalytic asymmetric aldol reaction of β-keto esters with formaldehyde promoted by a dinuclear Ni2-Schiff base complex

Chemical Communications ◽

10.1039/b912380f ◽

2009 ◽

pp. 5138 ◽

Cited By ~ 53

Author(s):

Shinsuke Mouri ◽

Zhihua Chen ◽

Shigeki Matsunaga ◽

Masakatsu Shibasaki

Keyword(s):

Schiff Base ◽

Aldol Reaction ◽

Schiff Base Complex ◽

Asymmetric Aldol ◽

Base Complex ◽

Keto Esters ◽

Asymmetric Aldol Reaction ◽

Catalytic Asymmetric

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Development of Highly Diastereo- and Enantioselective Direct Asymmetric Aldol Reaction of a Glycinate Schiff Base with Aldehydes Catalyzed by Chiral Quaternary Ammonium Salts

Journal of the American Chemical Society ◽

10.1021/ja048865q ◽

2004 ◽

Vol 126 (31) ◽

pp. 9685-9694 ◽

Cited By ~ 112

Author(s):

Takashi Ooi ◽

Minoru Kameda ◽

Mika Taniguchi ◽

Keiji Maruoka

Keyword(s):

Schiff Base ◽

Quaternary Ammonium ◽

Aldol Reaction ◽

Quaternary Ammonium Salts ◽

Ammonium Salts ◽

Asymmetric Aldol ◽

Asymmetric Aldol Reaction

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ChemInform Abstract: Direct Catalytic Asymmetric Aldol Reaction of Î²-Keto Esters with Formaldehyde Promoted by a Dinuclear Ni2-Schiff Base Complex.

ChemInform ◽

10.1002/chin.201001025 ◽

2010 ◽

Vol 41 (1) ◽

pp. no-no

Author(s):

Shinsuke Mouri ◽

Zhihua Chen ◽

Shigeki Matsunaga ◽

Masakatsu Shibasaki

Keyword(s):

Schiff Base ◽

Aldol Reaction ◽

Schiff Base Complex ◽

Asymmetric Aldol ◽

Base Complex ◽

Keto Esters ◽

Asymmetric Aldol Reaction ◽

Catalytic Asymmetric

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Development of Highly Diastereo- and Enantioselective Direct Asymmetric Aldol Reaction of a Glycinate Schiff Base with Aldehydes Catalyzed by Chiral Quaternary Ammonium Salts.

ChemInform ◽

10.1002/chin.200447059 ◽

2004 ◽

Vol 35 (47) ◽

Author(s):

Takashi Ooi ◽

Minoru Kameda ◽

Mika Taniguchi ◽

Keiji Maruoka

Keyword(s):

Schiff Base ◽

Quaternary Ammonium ◽

Aldol Reaction ◽

Quaternary Ammonium Salts ◽

Ammonium Salts ◽

Asymmetric Aldol ◽

Asymmetric Aldol Reaction

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Dual Proline/Water Compatible Lewis Acid Activation: a Biomimetic Approach for Direct Asymmetric Aldol Reaction

10.3390/ecsoc-13-00193 ◽

2009 ◽

Author(s):

Maël Penhoat ◽

Christian Rolando ◽

Didier Barbry

Keyword(s):

Lewis Acid ◽

Aldol Reaction ◽

Acid Activation ◽

Asymmetric Aldol ◽

Asymmetric Aldol Reaction ◽

Biomimetic Approach

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Recent Advances in Asymmetric Aldol Reaction of Masked Acetoacetic Esters Promoted by Ti(IV) / BINOL: A New Methodology, Non-Linear Effects and Autoinduction

Current Organic Chemistry ◽

10.2174/1385272043370212 ◽

2004 ◽

Vol 8 (11) ◽

pp. 993-1007 ◽

Cited By ~ 45

Author(s):

Soriente A. ◽

De M. ◽

Villano R. ◽

Scettri A.

Keyword(s):

Aldol Reaction ◽

Asymmetric Aldol ◽

Recent Advances ◽

Asymmetric Aldol Reaction ◽

Non Linear ◽

Linear Effects

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ChemInform Abstract: Asymmetric Aldol Reaction of Dichloroacetaldehyde Catalyzed by Diarylprolinol.

ChemInform ◽

10.1002/chin.201649067 ◽

2016 ◽

Vol 47 (49) ◽

Author(s):

Yujiro Hayashi ◽

Daichi Nakamura ◽

Yusuke Yasui ◽

Kotaro Iwasaki ◽

Hiroaki Chiba

Keyword(s):

Aldol Reaction ◽

Asymmetric Aldol ◽

Asymmetric Aldol Reaction

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Direct asymmetric aldol reaction in continuous flow using gel‐bound organocatalysts

European Journal of Organic Chemistry ◽

10.1002/ejoc.202100268 ◽

2021 ◽

Author(s):

Carsten J. Schmiegel ◽

Rene Baier ◽

Dirk Kuckling

Keyword(s):

Continuous Flow ◽

Aldol Reaction ◽

Asymmetric Aldol ◽

Asymmetric Aldol Reaction

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